Variant report

Variant	nsv898424
Chromosome Location	chr11:121108865-121206354
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1885)
CpG islands
(count:1346)
Chromatin interactive
region (count:47)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1885 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:121128072-121128368	K562	blood:	n/a	n/a
2	ARID3A	chr11:121163127-121163610	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:121120083-121120098	K562	blood:	n/a	n/a
4	ARID3A	chr11:121164256-121164604	K562	blood:	n/a	n/a
5	ATF1	chr11:121127953-121128343	K562	blood:	n/a	n/a
6	ATF1	chr11:121163106-121163710	K562	blood:	n/a	n/a
7	ATF2	chr11:121162582-121163636	GM12878	blood:	n/a	n/a
8	ATF2	chr11:121180245-121181179	GM12878	blood:	n/a	n/a
9	ATF2	chr11:121163055-121163491	GM12878	blood:	n/a	n/a
10	ATF2	chr11:121162992-121163490	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr11:121169426-121169836	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr11:121128039-121128392	K562	blood:	n/a	n/a
13	ATF3	chr11:121163116-121163588	H1-hESC	embryonic stem cell:	n/a	chr11:121163336-121163356 chr11:121163347-121163367
14	ATF3	chr11:121163059-121163538	GM12878	blood:	n/a	chr11:121163336-121163356 chr11:121163347-121163367
15	ATF3	chr11:121163257-121163429	GM12878	blood:	n/a	chr11:121163336-121163356 chr11:121163347-121163367
16	ATF3	chr11:121163186-121163470	K562	blood:	n/a	chr11:121163336-121163356 chr11:121163347-121163367
17	ATF3	chr11:121163174-121163514	HepG2	liver:	n/a	chr11:121163336-121163356 chr11:121163347-121163367
18	ATF3	chr11:121163124-121163504	H1-hESC	embryonic stem cell:	n/a	chr11:121163336-121163356 chr11:121163347-121163367
19	BACH1	chr11:121163265-121163401	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr11:121153833-121154109	GM12878	blood:	n/a	n/a
21	BATF	chr11:121153907-121154225	GM12878	blood:	n/a	n/a
22	BATF	chr11:121108683-121109269	GM12878	blood:	n/a	n/a
23	BATF	chr11:121108727-121109060	GM12878	blood:	n/a	n/a
24	BCL11A	chr11:121180383-121180787	GM12878	blood:	n/a	n/a
25	BCL11A	chr11:121108704-121109088	GM12878	blood:	n/a	n/a
26	BCL11A	chr11:121108685-121109034	GM12878	blood:	n/a	n/a
27	BCLAF1	chr11:121180306-121180890	GM12878	blood:	n/a	n/a
28	BCLAF1	chr11:121162869-121163527	GM12878	blood:	n/a	chr11:121163500-121163513 chr11:121163505-121163514
29	BCLAF1	chr11:121119932-121120167	GM12878	blood:	n/a	n/a
30	BHLHE40	chr11:121128050-121128347	K562	blood:	n/a	n/a
31	BHLHE40	chr11:121162938-121164079	K562	blood:	n/a	n/a
32	BHLHE40	chr11:121163101-121163660	GM12878	blood:	n/a	n/a
33	BHLHE40	chr11:121163075-121163794	HepG2	liver:	n/a	n/a
34	BHLHE40	chr11:121189749-121190235	K562	blood:	n/a	n/a
35	BHLHE40	chr11:121119971-121120171	GM12878	blood:	n/a	n/a
36	BHLHE40	chr11:121180381-121180770	GM12878	blood:	n/a	n/a
37	BRCA1	chr11:121162939-121163503	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr11:121193841-121194165	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr11:121163783-121163957	HepG2	liver:	n/a	n/a
40	BRCA1	chr11:121163232-121163509	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr11:121162946-121163052	HepG2	liver:	n/a	n/a
42	BRCA1	chr11:121163285-121163407	HepG2	liver:	n/a	n/a
43	BRCA1	chr11:121162845-121163300	GM12878	blood:	n/a	n/a
44	BRCA1	chr11:121164140-121164649	Hela-S3	cervix:	n/a	n/a
45	CBX3	chr11:121116609-121116968	K562	blood:	n/a	n/a
46	CBX3	chr11:121163035-121163575	K562	blood:	n/a	n/a
47	CCNT2	chr11:121127986-121128421	K562	blood:	n/a	n/a
48	CCNT2	chr11:121163185-121164015	K562	blood:	n/a	n/a
49	CEBPB	chr11:121163851-121164362	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr11:121163146-121163525	Hela-S3	cervix:	n/a	chr11:121163422-121163430

(count:1346 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:121163254-121163304	GM12892	blood:	n/a
2	chr11:121159792-121159842	HNPCEpiC	eye:	n/a
3	chr11:121112773-121112823	BJ	skin:	n/a
4	chr11:121163951-121164001	SAEC	small airway:	n/a
5	chr11:121163254-121163304	GM12892	blood:	n/a
6	chr11:121159792-121159842	HNPCEpiC	eye:	n/a
7	chr11:121112773-121112823	BJ	skin:	n/a
8	chr11:121163951-121164001	SAEC	small airway:	n/a
9	chr11:121193898-121193948	Hela-S3	cervix:	n/a
10	chr11:121162894-121162944	AG04449	skin:	fetal
11	chr11:121163951-121164001	HRCEpiC	kidney:	n/a
12	chr11:121126488-121126538	SK-N-SH	brain:	n/a
13	chr11:121163419-121163469	PFSK-1	brain:	n/a
14	chr11:121126488-121126538	ProgFib	skin:	n/a
15	chr11:121163095-121163145	AG10803	skin:	n/a
16	chr11:121163394-121163444	HEK293	kidney:	embryo
17	chr11:121163394-121163444	T-47D	breast:	n/a
18	chr11:121163419-121163469	HMEC	breast:	n/a
19	chr11:121179693-121179743	HRPEpiC	eye:	n/a
20	chr11:121163419-121163469	HIPEpiC	eye:	n/a
21	chr11:121163141-121163191	IMR90	lung:	fetal
22	chr11:121163095-121163145	HPAEpiC	pulmonary alveolar:	n/a
23	chr11:121163245-121163295	NT2-D1	testis:	n/a
24	chr11:121174513-121174563	RPTEC	kidney:	n/a
25	chr11:121163394-121163444	SK-N-SH	brain:	n/a
26	chr11:121163419-121163469	AoSMC	blood vessel:	n/a
27	chr11:121163254-121163304	Jurkat	blood:	n/a
28	chr11:121162894-121162944	NHBE	bronchial:	n/a
29	chr11:121193898-121193948	SK-N-SH	brain:	n/a
30	chr11:121163095-121163145	AG04450	lung:	fetal
31	chr11:121162894-121162944	SKMC	muscle:	n/a
32	chr11:121163245-121163295	NB4	blood:	n/a
33	chr11:121139309-121139359	AG09309	skin:	n/a
34	chr11:121163419-121163469	GM06990	blood:	n/a
35	chr11:121162894-121162944	RPTEC	kidney:	n/a
36	chr11:121193898-121193948	HCF	heart:	n/a
37	chr11:121163509-121163559	MCF-7	breast:	n/a
38	chr11:121163434-121163484	HAEpiC	amniotic membrane:	n/a
39	chr11:121193898-121193948	AG10803	skin:	n/a
40	chr11:121163419-121163469	NH-A	brain:	n/a
41	chr11:121163141-121163191	H1-hESC	embryonic stem cell:	embryo
42	chr11:121163447-121163497	HIPEpiC	eye:	n/a
43	chr11:121159792-121159842	HL-60	blood:	n/a
44	chr11:121172924-121172974	GM12878	blood:	n/a
45	chr11:121163447-121163497	SK-N-MC	brain:	n/a
46	chr11:121163434-121163484	GM12878	blood:	n/a
47	chr11:121163108-121163158	K562	blood:	n/a
48	chr11:121139309-121139359	AG04449	skin:	fetal
49	chr11:121126488-121126538	AoSMC	blood vessel:	n/a
50	chr11:121163394-121163444	SK-N-MC	brain:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:121123220..121124727-chr11:121126741..121128894,2	MCF-7	breast:
2	chr11:121162094..121164692-chr11:121196782..121198329,2	MCF-7	breast:
3	chr11:121119550..121120309-chr11:121128695..121129440,2	MCF-7	breast:
4	chr11:121163462..121165010-chr11:121166449..121168462,2	K562	blood:
5	chr11:121179024..121181756-chr11:121184079..121185753,2	MCF-7	breast:
6	chr11:121191941..121192910-chr11:121404447..121405457,5	MCF-7	breast:
7	chr11:121138852..121140402-chr11:121150063..121152826,2	MCF-7	breast:
8	chr11:121168682..121170319-chr11:121173753..121175738,2	MCF-7	breast:
9	chr11:121175030..121177296-chr11:121177510..121179226,2	MCF-7	breast:
10	chr11:121120979..121124837-chr11:121162716..121167264,4	MCF-7	breast:
11	chr11:121143746..121145252-chr11:121162829..121165757,2	MCF-7	breast:
12	chr11:121163184..121163771-chr7:116594188..116594742,2	HCT-116	colon:
13	chr11:121165737..121167537-chr11:121172249..121174931,2	MCF-7	breast:
14	chr11:121135011..121137028-chr11:121164041..121166376,2	K562	blood:
15	chr10:118414207..118414816-chr11:121128394..121128902,2	MCF-7	breast:
16	chr11:121183918..121185810-chr11:121187037..121189275,2	K562	blood:
17	chr11:121097383..121099804-chr11:121109722..121112130,2	K562	blood:
18	chr11:121189831..121190442-chr11:121461888..121462730,2	MCF-7	breast:
19	chr11:121119963..121121540-chr11:121162241..121164433,2	MCF-7	breast:
20	chr11:121183918..121185810-chr11:121187037..121189275,2	K562	blood:
21	chr11:121196619..121198318-chr11:121319649..121321226,2	MCF-7	breast:
22	chr11:121119550..121120309-chr11:121128695..121129440,2	MCF-7	breast:
23	chr11:121165790..121168233-chr11:121171467..121173048,2	K562	blood:
24	chr11:121189964..121190649-chr11:121404609..121405478,2	MCF-7	breast:
25	chr11:121128907..121131227-chr11:121168561..121171348,2	MCF-7	breast:
26	chr11:121116144..121118491-chr11:121120559..121122372,2	K562	blood:
27	chr11:121179024..121181756-chr11:121184079..121185753,2	MCF-7	breast:
28	chr11:121126834..121128836-chr11:121162575..121164973,2	MCF-7	breast:
29	chr11:121135011..121137028-chr11:121164041..121166376,2	K562	blood:
30	chr11:121138852..121140402-chr11:121150063..121152826,2	MCF-7	breast:
31	chr11:121192033..121192612-chr11:121461567..121462290,2	MCF-7	breast:
32	chr11:121156064..121158303-chr11:121162693..121164351,2	K562	blood:
33	chr11:121119672..121120581-chr11:121205492..121206275,2	MCF-7	breast:
34	chr11:121120979..121124837-chr11:121162716..121167264,4	MCF-7	breast:
35	chr11:121162777..121166095-chr11:121169824..121173301,4	MCF-7	breast:
36	chr11:121119672..121120581-chr11:121205492..121206275,2	MCF-7	breast:
37	chr11:121134743..121136689-chr11:121161761..121164688,2	MCF-7	breast:
38	chr11:121128907..121131227-chr11:121168561..121171348,2	MCF-7	breast:
39	chr11:121165790..121168233-chr11:121171467..121173048,2	K562	blood:
40	chr11:121173775..121175473-chr11:121177046..121178773,2	K562	blood:
41	chr11:121165737..121167537-chr11:121172249..121174931,2	MCF-7	breast:
42	chr11:121163283..121164037-chr15:65596989..65597882,2	Hela-S3	cervix:
43	chr10:1711711..1712250-chr11:121192076..121192589,2	MCF-7	breast:
44	chr11:121152423..121155228-chr11:121161820..121163745,2	K562	blood:
45	chr11:121123220..121124727-chr11:121126741..121128894,2	MCF-7	breast:
46	chr11:121192094..121192920-chr11:121461877..121462689,3	MCF-7	breast:
47	chr11:121159131..121161602-chr11:121161646..121164535,3	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BLID-11	chr11:121120979-121121687	NONHSAT024739
2	lnc-BLID-10	chr11:121199675-121199796	NONHSAT024745
3	lnc-BLID-10	chr11:121198196-121198545	NONHSAT024745

No data

(count:1 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SC5DL	hsa-let-7b-5p	chr11:121177840-121177860

Variant related genes	Relation type
RPS4XP12	TF binding region
SC5D	TF binding region
ENSG00000254515	TF binding region
RPS4XP12	CpG island
SC5D	CpG island
ENSG00000254515	CpG island
ENSG00000244400	chromatin interactions
ENSG00000004866	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000227199	chromatin interactions
ENSG00000214188	chromatin interactions
ENSG00000109929	chromatin interactions

Extended variants
information (count: 3818 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:3818 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1941298	chr11:121108865-121108866	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551688690	chr11:121108881-121108882	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs113548316	chr11:121108885-121108886	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs112104532	chr11:121108895-121108896	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs113634036	chr11:121108900-121108901	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs1941299	chr11:121108907-121108908	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs555708293	chr11:121108913-121108914	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs371232071	chr11:121108952-121108953	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs544357333	chr11:121108962-121108963	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs574127672	chr11:121108981-121108982	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs540037304	chr11:121109046-121109047	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs548861768	chr11:121109088-121109089	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs535735989	chr11:121109135-121109136	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs554066499	chr11:121109149-121109150	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs572373025	chr11:121109150-121109151	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs545951097	chr11:121109200-121109201	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs564141023	chr11:121109214-121109215	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs558026169	chr11:121109235-121109236	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs576072195	chr11:121109246-121109247	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs543182064	chr11:121109359-121109360	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs561345084	chr11:121109363-121109364	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs528897886	chr11:121109364-121109365	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs570527554	chr11:121109394-121109395	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs71473189	chr11:121109425-121109426	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs547000765	chr11:121109438-121109439	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs6589864	chr11:121109489-121109490	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs146688614	chr11:121109514-121109515	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs556163197	chr11:121109525-121109526	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs11218217	chr11:121109530-121109531	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs11218218	chr11:121109536-121109537	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs11218219	chr11:121109539-121109540	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs11218220	chr11:121109546-121109547	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs11218221	chr11:121109550-121109551	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs533481309	chr11:121109560-121109561	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs376220547	chr11:121109561-121109562	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs372370314	chr11:121109572-121109573	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs34884998	chr11:121109580-121109581	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs397714955	chr11:121109581-121109582	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs139255230	chr11:121109606-121109607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570179465	chr11:121109621-121109622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs537545569	chr11:121109629-121109630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549547829	chr11:121109631-121109632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs557074207	chr11:121109642-121109643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567766022	chr11:121109653-121109654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542172908	chr11:121109657-121109658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs534977111	chr11:121109722-121109723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553420108	chr11:121109760-121109761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs75562111	chr11:121109782-121109783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs556077900	chr11:121109807-121109808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs539380266	chr11:121109809-121109810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	17327916	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Developmental delay	21147756	CNVD
Squamous cell cancer	20885788	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Neurocytoma	17123091	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Central neurocytomas	17123091	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	16750200	CNVD
Multiple myeloma	17550852	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Acute myeloid leukemia	19651601	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	20409316	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21509527	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21385341	CNVD
Multiple myeloma	16461302	CNVD
Burkitt''s lymphoma	18698080	CNVD
Prostate cancer	23792589	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Effusion lymphoma	18079361	CNVD
Chronic lymphocytic leukemia	17053054	CNVD

Chromatin state (count:1768 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:121104400-121109000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr11:121104400-121110600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:121104600-121109400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:121104600-121110000	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr11:121104600-121110200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:121104600-121113200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr11:121104800-121109200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr11:121104800-121113200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr11:121105600-121112800	Enhancers	Fetal Muscle Leg	muscle
10	chr11:121105800-121109000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr11:121105800-121113800	Enhancers	Muscle Satellite Cultured Cells	--
12	chr11:121106000-121110200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr11:121106600-121110400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr11:121106600-121112800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr11:121106800-121109000	Enhancers	NH-A	brain
16	chr11:121106800-121109600	Enhancers	NHEK	skin
17	chr11:121107000-121109400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr11:121107000-121109600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr11:121107400-121109400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr11:121107800-121111000	Weak transcription	Right Atrium	heart
21	chr11:121107800-121112000	Weak transcription	Liver	Liver
22	chr11:121107800-121112400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr11:121107800-121116800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr11:121108000-121109000	Enhancers	Osteobl	bone
25	chr11:121108000-121109400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr11:121108000-121110400	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr11:121108000-121111200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr11:121108000-121111600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr11:121108200-121109400	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr11:121108200-121109400	Flanking Active TSS	GM12878-XiMat	blood
31	chr11:121108200-121109400	Enhancers	HUVEC	blood vessel
32	chr11:121108200-121110600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr11:121108400-121109000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr11:121108400-121109200	Enhancers	Fetal Stomach	stomach
35	chr11:121108600-121109000	Enhancers	Primary B cells from peripheral blood	blood
36	chr11:121108600-121111000	Weak transcription	Esophagus	oesophagus
37	chr11:121108600-121111000	Weak transcription	Fetal Muscle Trunk	muscle
38	chr11:121108600-121111600	Enhancers	HSMM	muscle
39	chr11:121108600-121112000	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr11:121108600-121112000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr11:121108600-121112400	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr11:121108600-121116400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr11:121108800-121109000	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr11:121108800-121109200	Enhancers	HSMMtube	muscle
45	chr11:121109000-121109200	Flanking Active TSS	Osteobl	bone
46	chr11:121109000-121109400	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr11:121109000-121110400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr11:121109000-121110800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr11:121109200-121109600	Flanking Active TSS	HSMMtube	muscle
50	chr11:121109200-121109600	Enhancers	Osteobl	bone

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